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Kinetic studies on the interaction between EGFR and EGF and its traditional Chinese medicine-modulation by surface plasmon resonance

机译:关于EGFR和EGF之间相互作用及其中药调节的动力学研究

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Epidermal growth factor receptor (EGFR) is an important target on cancer therapy. One of the approaches is to modulate EGFR induced ligand-binding affinity change. In order to understand the correlation between ligand-binding change and EGFR modulation, we try to get some small molecular agents from traditional Chinese medicines (TCMs) to modulate EGFR activity on the biosensor system. Among 60 of TCMs, we find that some samples exhibit different influence on EGFR modulation. Among these, 051 showed a more inhibitive property due to decreasing EGF-affinity, -binding to EGFR and existed an anti-EGFR activity to A549 cells. On the other hand, 040 exist opposite function to 051. 040 is a most powerful enhancer that can increase the affinity and quantity of EGF binding to EGFR and a pro-EGFR activity on cell culture system. In our study, we can successfully regulate the EGFR-mediated cell proliferation and anti-apoptosis by modulating the affinity of EGF-EGFR interaction. This way will be a useful method to apply on the therapy of human diseases.
机译:表皮生长因子受体(EGFR)是癌症治疗的重要靶标。其中一种方法是调节EGFR诱导的配体结合亲和力变化。为了了解配体结合变化与EGFR调节之间的相关性,我们尝试从中药(TCMS)中获得一些小分子试剂,以调节生物传感器系统的EGFR活性。在60例TCM中,我们发现一些样品对EGFR调节表现出不同的影响。其中,由于降低EGF - 亲和力,051表现出更抑制的特性, - 缠绕至EGFR并将抗EGFR活性存在于A549细胞。另一方面,040存在对051的相反函数。040是一种最强大的增强剂,可以提高EGF与EGFR的亲和力和量和细胞培养系统上的预富普活性。在我们的研究中,我们可以通过调节EGF-EGFR相互作用的亲和力来成功调节EGFR介导的细胞增殖和抗细胞凋亡。这种方式将是申请人类疾病治疗的有用方法。

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